Literature DB >> 23636577

Hypophosphatemic rickets due to perturbations in renal tubular function.

Maria Goretti M G Penido1, Uri S Alon.   

Abstract

The common denominator for all types of rickets is hypophosphatemia, leading to inadequate supply of the mineral to the growing bone. Hypophosphatemia can result from insufficient uptake of the mineral from the gut or its disproportionate losses in the kidney, the latter being caused by either tubular abnormalities per se or the effect on the tubule of circulating factors like fibroblast growth factor-23 and parathyroid hormone (PTH). High serum levels of the latter result in most cases from abnormalities in vitamin D metabolism which lead to decreased calcium absorption in the gut and hypocalcemia, triggering PTH secretion. Rickets is a disorder of the growth plate and hence pediatric by definition. However, it is important to recognize that the effect of hypophosphatemia on other parts of the skeleton results in osteomalacia in both children and adults. This review addresses the etiology, pathophysiologic mechanisms, clinical manifestations and treatment of entities associated with hypophosphatemic rickets due to perturbations in renal tubular function.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23636577     DOI: 10.1007/s00467-013-2466-z

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  68 in total

1.  X-linked hypophosphatemia: effects of treatment with recombinant human growth hormone.

Authors:  G S Reusz; G Miltényi; G Stubnya; A Szabó; C Horváth; D J Byrd; F Péter; T Tulassay
Journal:  Pediatr Nephrol       Date:  1997-10       Impact factor: 3.714

Review 2.  FGF23 and the parathyroid glands.

Authors:  Justin Silver; Tally Naveh-Many
Journal:  Pediatr Nephrol       Date:  2010-06-05       Impact factor: 3.714

3.  Renal transplantation in hypophosphatemia with vitamin D-resistant rickets.

Authors:  J M Morgan; W L Hawley; A I Chenoweth; W J Retan; A G Diethelm
Journal:  Arch Intern Med       Date:  1974-09

Review 4.  Regulation of phosphate transport by fibroblast growth factor 23 (FGF23): implications for disorders of phosphate metabolism.

Authors:  Jyothsna Gattineni; Michel Baum
Journal:  Pediatr Nephrol       Date:  2009-08-11       Impact factor: 3.714

5.  Resolution of medullary nephrocalcinosis in children with metabolic bone disorders.

Authors:  Ari Auron; Uri S Alon
Journal:  Pediatr Nephrol       Date:  2005-06-23       Impact factor: 3.714

6.  Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder.

Authors:  M J Econs; P T McEnery
Journal:  J Clin Endocrinol Metab       Date:  1997-02       Impact factor: 5.958

7.  High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH.

Authors:  Junko Miyamoto Igaki; Makoto Yamada; Yuji Yamazaki; Shinobu Koto; Masako Izawa; Daisuke Ariyasu; Eri Suzuki; Hisashi Hasegawa; Yukihiro Hasegawa
Journal:  Endocr J       Date:  2011-05-19       Impact factor: 2.349

Review 8.  Overview of the FGF23-Klotho axis.

Authors:  Makoto Kuro-o
Journal:  Pediatr Nephrol       Date:  2009-07-22       Impact factor: 3.714

9.  Effects of hydrochlorothiazide and amiloride in renal hypophosphatemic rickets.

Authors:  U Alon; J C Chan
Journal:  Pediatrics       Date:  1985-04       Impact factor: 7.124

Review 10.  FGF-23 in bone biology.

Authors:  Katherine Wesseling-Perry
Journal:  Pediatr Nephrol       Date:  2009-12-15       Impact factor: 3.714

View more
  7 in total

Review 1.  FGF23 and Associated Disorders of Phosphate Wasting.

Authors:  Anisha Gohil; Erik A Imel
Journal:  Pediatr Endocrinol Rev       Date:  2019-09

Review 2.  Use of calcimimetics in children with normal kidney function.

Authors:  Judith Sebestyen VanSickle; Tarak Srivastava; Uri S Alon
Journal:  Pediatr Nephrol       Date:  2018-03-19       Impact factor: 3.714

3.  Dentoalveolar Abscesses Not Associated with Caries or Trauma: A Diagnostic Hallmark of Hypophosphatemic Rickets Initially Misdiagnosed as Hypochondroplasia.

Authors:  Silvia Elena Yacarini Paredes; Raquel Assed Bezerra Segato; Leila Daher Moreira; Alcides Moreira; Kranya Victoria Díaz Serrano; Clarissa Teles Rodrigues; Luciana Yamamoto Almeida; Jorge Esquiche León
Journal:  Head Neck Pathol       Date:  2017-11-30

4.  Osteopetrorickets due to Snx10 deficiency in mice results from both failed osteoclast activity and loss of gastric acid-dependent calcium absorption.

Authors:  Liang Ye; Leslie R Morse; Li Zhang; Hajime Sasaki; Jason C Mills; Paul R Odgren; Greg Sibbel; James R L Stanley; Gee Wong; Ariane Zamarioli; Ricardo A Battaglino
Journal:  PLoS Genet       Date:  2015-03-26       Impact factor: 5.917

Review 5.  Rickets guidance: part I-diagnostic workup.

Authors:  Dieter Haffner; Maren Leifheit-Nestler; Andrea Grund; Dirk Schnabel
Journal:  Pediatr Nephrol       Date:  2021-12-15       Impact factor: 3.651

6.  X-linked hypophosphatemic rickets: a new mutation.

Authors:  Patrícia Maio; Lia Mano; Sara Rocha; Rute Baeta Baptista; Telma Francisco; Helena Sousa; João Parente Freixo; Margarida Abranches
Journal:  J Bras Nefrol       Date:  2021 Apr-Jun

7.  Role of FGF23 in Pediatric Hypercalciuria.

Authors:  Maria Goretti Moreira Guimarães Penido; Marcelo de Sousa Tavares; Uri Saggie Alon
Journal:  Biomed Res Int       Date:  2017-12-31       Impact factor: 3.411

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.